Vidaud D - Search Results

1

Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis.

Louvrier C, Pasmant E, Briand-Suleau A, Cohen J, Nitschké P, Nectoux J, Orhant L, Zordan C, Goizet C, Goutagny S, Lallemand D, Vidaud M, Vidaud D, Kalamarides M, Parfait B. Louvrier C, et al. Among authors: vidaud m, vidaud d. Neuro Oncol. 2018 Jun 18;20(7):917-929. doi: 10.1093/neuonc/noy009. Neuro Oncol. 2018. PMID: 29409008 Free PMC article.

2

Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior.

Attree O, Vidaud D, Vidaud M, Amselem S, Lavergne JM, Goossens M. Attree O, et al. Among authors: vidaud m, vidaud d. Genomics. 1989 Apr;4(3):266-72. doi: 10.1016/0888-7543(89)90330-3. Genomics. 1989. PMID: 2714791

3

Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genes.

Bretagne S, Assouline B, Vidaud D, Houin R, Vidaud M. Bretagne S, et al. Among authors: vidaud m, vidaud d. Exp Parasitol. 1996 Apr;82(3):324-8. doi: 10.1006/expr.1996.0040. Exp Parasitol. 1996. PMID: 8631384 No abstract available.

4

Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome.

Bahuau M, Houdayer C, Assouline B, Blanchet-Bardon C, Le Merrer M, Lyonnet S, Giraud S, Récan D, Lakhdar H, Vidaud M, Vidaud D. Bahuau M, et al. Among authors: vidaud m, vidaud d. Am J Med Genet. 1998 Jan 23;75(3):265-72. Am J Med Genet. 1998. PMID: 9475595

5

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.

Bahuau M, Vidaud D, Jenkins RB, Bièche I, Kimmel DW, Assouline B, Smith JS, Alderete B, Cayuela JM, Harpey JP, Caille B, Vidaud M. Bahuau M, et al. Among authors: vidaud m, vidaud d. Cancer Res. 1998 Jun 1;58(11):2298-303. Cancer Res. 1998. PMID: 9622062

6

Novel approach to quantitative polymerase chain reaction using real-time detection: application to the detection of gene amplification in breast cancer.

Bièche I, Olivi M, Champème MH, Vidaud D, Lidereau R, Vidaud M. Bièche I, et al. Among authors: vidaud m, vidaud d. Int J Cancer. 1998 Nov 23;78(5):661-6. doi: 10.1002/(sici)1097-0215(19981123)78:5<661::aid-ijc22>3.0.co;2-i. Int J Cancer. 1998. PMID: 9808539

7

Quantitation of MYC gene expression in sporadic breast tumors with a real-time reverse transcription-PCR assay.

Bièche I, Laurendeau I, Tozlu S, Olivi M, Vidaud D, Lidereau R, Vidaud M. Bièche I, et al. Among authors: vidaud m, vidaud d. Cancer Res. 1999 Jun 15;59(12):2759-65. Cancer Res. 1999. PMID: 10383126

8

TaqMan PCR-based gene dosage assay for predictive testing in individuals from a cancer family with INK4 locus haploinsufficiency.

Laurendeau I, Bahuau M, Vodovar N, Larramendy C, Olivi M, Bieche I, Vidaud M, Vidaud D. Laurendeau I, et al. Among authors: vidaud m, vidaud d. Clin Chem. 1999 Jul;45(7):982-6. Clin Chem. 1999. PMID: 10388473

9

Somatic mosaicism and compound heterozygosity in female hemophilia B.

Costa JM, Vidaud D, Laurendeau I, Vidaud M, Fressinaud E, Moisan JP, David A, Meyer D, Lavergne JM. Costa JM, et al. Among authors: vidaud m, vidaud d. Blood. 2000 Aug 15;96(4):1585-7. Blood. 2000. PMID: 10942410 Free article.

10

Human TIP49b/RUVBL2 gene: genomic structure, expression pattern, physical link to the human CGB/LHB gene cluster on chromosome 19q13.3.

Parfait B, Giovangrandi Y, Asheuer M, Laurendeau I, Olivi M, Vodovar N, Vidaud D, Vidaud M, Bièche I. Parfait B, et al. Among authors: vidaud m, vidaud d. Ann Genet. 2000 Apr-Jun;43(2):69-74. doi: 10.1016/s0003-3995(00)01016-9. Ann Genet. 2000. PMID: 10998447

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